@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP532218.RAE1uZItQfT4QAHC2EZRKn-q2ySPCc99B86L008rVL3OE> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP532218.RAE1uZItQfT4QAHC2EZRKn-q2ySPCc99B86L008rVL3OE130_head {
  this: np:hasAssertion dgn-np:NP532218.RAE1uZItQfT4QAHC2EZRKn-q2ySPCc99B86L008rVL3OE130_assertion;
    np:hasProvenance dgn-np:NP532218.RAE1uZItQfT4QAHC2EZRKn-q2ySPCc99B86L008rVL3OE130_provenance;
    np:hasPublicationInfo dgn-np:NP532218.RAE1uZItQfT4QAHC2EZRKn-q2ySPCc99B86L008rVL3OE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP532218.RAE1uZItQfT4QAHC2EZRKn-q2ySPCc99B86L008rVL3OE130_assertion a np:Assertion .
  
  dgn-np:NP532218.RAE1uZItQfT4QAHC2EZRKn-q2ySPCc99B86L008rVL3OE130_provenance a np:Provenance .
  
  dgn-np:NP532218.RAE1uZItQfT4QAHC2EZRKn-q2ySPCc99B86L008rVL3OE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP532218.RAE1uZItQfT4QAHC2EZRKn-q2ySPCc99B86L008rVL3OE130_assertion {
  miriam-gene:6329 a ncit:C16612 .
  
  lld:C0086525 a ncit:C7057 .
  
  dgn-gda:DGNe2080be1a7ede269baa910956d50bcf9 sio:SIO_000628 miriam-gene:6329, lld:C0086525;
    a sio:SIO_001121 .
}

dgn-np:NP532218.RAE1uZItQfT4QAHC2EZRKn-q2ySPCc99B86L008rVL3OE130_provenance {
  dgn-np:NP532218.RAE1uZItQfT4QAHC2EZRKn-q2ySPCc99B86L008rVL3OE130_assertion dcterms:description
      "[The periodic paralyses are a group of autosomal dominant muscle diseases sharing the common feature of episodic stiffness and weakness, usually occurring with muscle cooling (as in the case of paramyotonia congenita, PC phenotype) or changes in extracellular K+ levels resulting from various precipitating factors (hyperkalemic periodic paralysis, HYPP and hypokalemic periodic paralysis, HypoPP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:7721550;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP532218.RAE1uZItQfT4QAHC2EZRKn-q2ySPCc99B86L008rVL3OE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:21+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}